Components from spider venom activate macrophages against glioblastoma cells: new potential adjuvants for anticancer immunotherapy

Author:

Munhoz Jaqueline1ORCID,Peron Gabriela2,Bonfanti Amanda Pires12,Oliveira Janine2,da Rocha-e-Silva Thomaz A A3,Sutti Rafael4,Thomé Rodolfo25,Bombeiro André Luís2,Barreto Natalia12,Chalbatani Ghanbar Mahmoodi6,Gharagouzloo Elahe7,Vitorino-Araujo João Luiz8,Verinaud Liana2,Rapôso Catarina1

Affiliation:

1. Faculdade de Ciências Farmacêuticas, Universidade Estadual de Campinas (UNICAMP). Cândido Portinari, 200 - Cidade Universitária, Campinas, São Paulo, 13083-871, Brazil

2. Departamento de Biologia Estrutural e Funcional, Instituto de Biologia, UNICAMP. Av. Bertrand Russel, Campinas, São Paulo, 13083-865, Brazil

3. Faculdade Israelita de Ciências da Saúde Albert Einstein, São Paulo, SP, 05652-900, Brazil

4. Faculdade de Ciências Médicas, Santa Casa de São Paulo. Dr. Cesário Motta Jr., 61, Vila Buarque, São Paulo, SP, 01221-020, Brazil

5. Department of Neurology, Thomas Jefferson University, 909 Walnut St #3, Philadelphia, PA, 19107, USA

6. Department of Immunology and Biology, TUMS School of Medicine, Poursina Road, Tehran, 1417613151, Iran

7. Cancer Institute, Keshavarz Blvd, Tehran University of Medical Science, Tehran, 1419733141, Iran

8. Disciplina de Neurocirurgia, Faculdade de Ciências Médicas da Santa Casa de São Paulo. Dona Veridiana, 56 - Higienópolis, São Paulo - SP, 01238-010, Brazil

Abstract

Abstract Immunomodulation has been considered an important approach in the treatment of malignant tumours. However, the modulation of innate immune cells remains an underexplored tool. Studies from our group demonstrated that the Phoneutria nigriventer spider venom (PnV) administration increased the infiltration of macrophage in glioblastoma, in addition to decreasing the tumour size in a preclinical model. The hypothesis that PnV would be modulating the innate immune system led us to the main objective of the present study: to elucidate the effects of PnV and its purified fractions on cultured macrophages. Results showed that PnV and the three fractions activated macrophages differentiated from bone marrow precursors. Further purification generated 23 subfractions named low weight (LW-1 to LW-12) and high weight (HW-1 to HW-11). LW-9 presented the best immunomodulatory effect. Treated cells were more phagocytic, migrated more, showed an activated morphological profile and induced an increased cytotoxic effect of macrophages on tumour cells. However, while M1-controls (LPS) increased IL-10, TNF-alpha and IL-6 release, PnV, fractions and subfractions did not alter any cytokine, with the exception of LW-9 that stimulated IL-10 production. These findings suggest that molecules present in LW-9 have the potential to be used as immunoadjuvants in the treatment of cancer.

Funder

Cytation TM Cell Imaging Multi-Mode Reader

Multi-User Equipment Program

São Paulo Research Foundation

Brazilian foundations: Fundação de Amparo à Pesquisa do Estado de São Paulo (the São Paulo Research Foundation—FAPESP—Grant

Conselho Nacional de Desenvolvimento Científco e Tecnológico (the Brazilian National Council for Scientific and Technological Development—CNPq—Grant

FAPESP

CNPq

Publisher

Oxford University Press (OUP)

Subject

Molecular Biology,Biochemistry,General Medicine

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